Hyperkisspeptinemia and Hypothalamic-Pituitary-Gonadal Axis Uncoupling in Hemodialysis Patients: Clinical Evidence Suggestive of Central Desensitization

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ID: 323003
2026
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Abstract
Abstract Background Reproductive and sexual dysfunction (uremic hypogonadism) are pervasive in maintenance hemodialysis (MHD) patients, yet the underlying neuroendocrine mechanisms remain poorly understood. Kisspeptin is the master upstream regulator of the hypothalamic-pituitary-gonadal (HPG) axis. We hypothesized that uremia-induced kisspeptin accumulation is associated with HPG axis uncoupling through central desensitization. Methods In this cross-sectional study, 69 MHD patients and 20 age-matched healthy controls (HC) were recruited. All participants were rigorously screened to exclude active inflammation and primary gonadal disease. Serum kisspeptin, gonadotropins, and sex steroids were quantified. Mediation analysis was performed to elucidate the pathophysiological pathway between kisspeptin and erectile dysfunction (ED) in males. Results Serum kisspeptin was profoundly elevated in MHD patients versus HCs (median, 30.35 vs. 9.02 ng/mL; P < 0.001). In uremic females, despite profound hypoestrogenism and massive kisspeptin stimuli, compensatory gonadotropin surges were blunted (FSH: P = 0.138; LH: P = 0.149), suggesting potential pituitary desensitization. In uremic males, kisspeptin independently predicted decreased testosterone (β = -0.045, P = 0.046) after adjusting for age, CRP, and diabetes. Mediation analysis revealed a mediation pattern consistent with testosterone-mediated effects of kisspeptin’s impact on erectile function (indirect effect P = 0.046; direct effect P = 0.081), suggesting that kisspeptin accumulation may be associated with ED exclusively by suppressing the HPG axis. Serum kisspeptin predicted moderate-to-severe ED (AUC 0.734, 95% CI: 0.596–0.872). Conclusions The marked hyperkisspeptinemia and concurrent HPG axis uncoupling observed in uremic patients are clinically suggestive of central neuroendocrine desensitization. Serum kisspeptin may serve as a novel exploratory functional proxy for the severity of uremic endocrine disruption, offering a potential target for therapeutic intervention.
Reference Key
openalex_W7171836986 Use this key to autocite in the manuscript while using SciMatic Manuscript Manager or Thesis Manager
Authors Naiying Lan, Dan Ye, Maoting Li, Fanzhou Zeng, Cheng Xue, Zewei Chen, Qing Shao, Jun Liu, N. L. Liu, Bo Yang
Journal clinical kidney journal
Year 2026
DOI
10.1093/ckj/sfag238
URL
https://doi.org/10.1093/ckj/sfag238
Keywords Keywords not found

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